3.

The person responsible for the placing on the market of such a treated article shall ensure that the label provides the information listed in the second subparagraph, where: in the case of a treated article containing a biocidal product, a claim is made by the manufacturer of that treated article regarding the biocidal properties of the article, or in relation to the active substance(s) concerned, having particular regard to the possibility of contact with humans or the release into the environment, the conditions associated with the approval of the active substance(s) so require. The label referred to in the first subparagraph shall provide the following information: a statement that the treated article incorporates biocidal products; where substantiated, the biocidal property attributed to the treated article; without prejudice to Article 24 of Regulation (EC) No 1272/2008, the name of all active substances contained in the biocidal products; the name of all nanomaterials contained in the biocidal products, followed by the word ‘nano’ in brackets; any relevant instructions for use, including any precautions to be taken because of the biocidal products with which a treated article was treated or which it incorporates. This paragraph shall not apply where at least equivalent labelling requirements already exist under sector-specific legislation for biocidal products in treated articles to meet information requirements concerning those active substances.

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Source: EUR-Lex (Cellar) · retrieved 2026-10-29 · Text as adopted (Official Journal); later amendments are not incorporated in this text.